Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.37 (A)
Location

Chromosome 5:126543216 (forward strand)|View in location tab

Co-located variant

dbSNP rs199550747 (C/-)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58192485

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2506 sample genotypes.

Variant displays